Bivalent Vaccine Coverage
During September 4, 2022March 4, 2023, among 12,706,176 immunocompetent Medicare beneficiaries aged 65 years who had previously received an original COVID19 vaccine, 5,683,208 (44.7%) received a bivalent dose (Table 1). Overall, higher percentages of bivalent vaccine recipients than nonrecipients resided in an urban area (83% versus 78%), had received an influenza vaccine during the 202122 season (82% versus 55%) and 202223 season (87% versus 50%), and had received an original monovalent booster vaccine dose (96% versus 73%).
Among 78,618 Medicare beneficiaries aged 18 years with ESRD receiving dialysis who did not have additional immunocompromising conditions and had previously received original COVID-19 vaccine, 23,229 (29.5%) received a bivalent dose, including 7,239 (31.2%) aged 1864 years and 15,990 (68.8%) aged 65 years. Similar to beneficiaries aged 65 years, among recipients with ESRD receiving dialysis, a higher percentage of those who received a bivalent vaccine dose compared with those who had not, had also received an influenza vaccine during the 202122 season (90% versus 82%) and the 202223 season (92% versus 79%) and had received an original monovalent booster vaccine dose (90% versus 74%). In addition, a higher percentage of bivalent COVID-19vaccinated ESRD beneficiaries were older (69% were aged 65 years) and non-Hispanic White (53%) compared with those who did not receive the bivalent COVID-19 vaccine (59% and 47%, respectively).
During the study period, COVID-19related thromboembolic events were recorded among 22,001 immunocompetent beneficiaries aged 65 years and 1,040 immunocompetent beneficiaries aged 18 years with ESRD receiving dialysis (Table 2). A total of 1,505,533,898 original-vaccineonly person-days were contributed by immunocompetent beneficiaries aged 65 years, during which 17,746 COVID-19related thromboembolic events were identified (Table 3). Among adults aged 65 years, 694,184,995 bivalent-vaccine person-days were contributed, during which 4,255 COVID-19related thromboembolic events were identified. Adjusted VE against COVID-19related thromboembolic events among immunocompetent beneficiaries aged 65 years was 47%, with lower VE estimates 60 days after bivalent vaccine receipt (42%) compared with VE estimates 759 days after bivalent vaccine receipt (54%).
Similarly, a total of 10,395,534 original-vaccine-only person-days were contributed by beneficiaries aged 18 years with ESRD receiving dialysis, during which 917 COVID-19related thromboembolic events were identified. A total of 2,394,731 bivalent vaccine person-days were contributed, during which 123 COVID-19related thromboembolic events were identified. Adjusted VE against COVID-19related thromboembolic events was 51%, with lower VE estimates 60 days after bivalent vaccine receipt (45%) than 759 days after bivalent vaccine receipt (56%); however, these differences were not statistically significant (i.e., the 95% CIs overlapped).
Similar results were seen among beneficiaries aged 65 years with immunocompromise (overall bivalent VE=46%, with 55% VE 759 days after receipt of vaccine, and 39% VE 60 days post-vaccination) and among beneficiaries with ESRD receiving dialysis and who had additional immunocompromising conditions (overall bivalent VE=45%, with 60% VE 759 days after receipt of vaccine, and nonsignificant 30% VE at 60 days post-vaccination) (Supplementary Table 1; https://stacks.cdc.gov/view/cdc/140316). A supplementary analysis estimating VE against all-cause thromboembolic events also indicated a protective effect of bivalent vaccination (Supplementary Table 2; https://stacks.cdc.gov/view/cdc/140315).
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